Jobs at Ergomed

Conducts on-site and remote monitoring visits for clinical trials, including pre-study, initiation, interim, and close-out activities. Verifies investigator and site qualifications, trains site personnel, supports regulatory and ethics committee submissions, and mentors junior clinical research staff through co-monitoring visits. Requires extensive phase 2/3 monitoring experience, preferably in oncology or rare disease trials, strong communication skills, English proficiency, and national travel availability.

Manages pharmacovigilance projects as the primary client contact, defining scope and objectives, planning activities and milestones, managing expectations, and preparing client and internal reports. Requires hands-on experience with pharmacovigilance activities including ICSR processing and review, aggregate reporting, literature screening, reconciliation, and SOP preparation. The role also involves senior stakeholder communication, leadership, mentoring, meeting facilitation, and problem solving.

Generates and qualifies prospects for pharmacovigilance and clinical-trial services. Responsibilities include researching leads, conducting outreach, nurturing marketing leads, supporting targeted campaigns, scheduling meetings, preparing early engagement presentations, facilitating RFPs, maintaining CRM information, and transferring qualified opportunities to sales team members. The role collaborates across sales and marketing teams while meeting quarterly and annual business development targets.